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Up-regulation of the Cdc42 GTPase limits the replicative life span of budding yeast
Cdc42, a conserved Rho GTPase, plays a central role in polarity establishment in yeast and animals. Cell polarity is critical for asymmetric cell division, and asymmetric cell division underlies replicative aging of budding yeast. Yet how Cdc42 and other polarity factors impact life span is largely...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The American Society for Cell Biology
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9250358/ https://www.ncbi.nlm.nih.gov/pubmed/35044837 http://dx.doi.org/10.1091/mbc.E21-04-0208 |
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author | Kang, Pil Jung Mullner, Rachel Li, Haoyu Hansford, Derek Shen, Han-Wei Park, Hay-Oak |
author_facet | Kang, Pil Jung Mullner, Rachel Li, Haoyu Hansford, Derek Shen, Han-Wei Park, Hay-Oak |
author_sort | Kang, Pil Jung |
collection | PubMed |
description | Cdc42, a conserved Rho GTPase, plays a central role in polarity establishment in yeast and animals. Cell polarity is critical for asymmetric cell division, and asymmetric cell division underlies replicative aging of budding yeast. Yet how Cdc42 and other polarity factors impact life span is largely unknown. Here we show by live-cell imaging that the active Cdc42 level is sporadically elevated in wild type during repeated cell divisions but rarely in the long-lived bud8 deletion cells. We find a novel Bud8 localization with cytokinesis remnants, which also recruit Rga1, a Cdc42 GTPase activating protein. Genetic analyses and live-cell imaging suggest that Rga1 and Bud8 oppositely impact life span likely by modulating active Cdc42 levels. An rga1 mutant, which has a shorter life span, dies at the unbudded state with a defect in polarity establishment. Remarkably, Cdc42 accumulates in old cells, and its mild overexpression accelerates aging with frequent symmetric cell divisions, despite no harmful effects on young cells. Our findings implicate that the interplay among these positive and negative polarity factors limits the life span of budding yeast. |
format | Online Article Text |
id | pubmed-9250358 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The American Society for Cell Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-92503582022-07-07 Up-regulation of the Cdc42 GTPase limits the replicative life span of budding yeast Kang, Pil Jung Mullner, Rachel Li, Haoyu Hansford, Derek Shen, Han-Wei Park, Hay-Oak Mol Biol Cell Brief Reports Cdc42, a conserved Rho GTPase, plays a central role in polarity establishment in yeast and animals. Cell polarity is critical for asymmetric cell division, and asymmetric cell division underlies replicative aging of budding yeast. Yet how Cdc42 and other polarity factors impact life span is largely unknown. Here we show by live-cell imaging that the active Cdc42 level is sporadically elevated in wild type during repeated cell divisions but rarely in the long-lived bud8 deletion cells. We find a novel Bud8 localization with cytokinesis remnants, which also recruit Rga1, a Cdc42 GTPase activating protein. Genetic analyses and live-cell imaging suggest that Rga1 and Bud8 oppositely impact life span likely by modulating active Cdc42 levels. An rga1 mutant, which has a shorter life span, dies at the unbudded state with a defect in polarity establishment. Remarkably, Cdc42 accumulates in old cells, and its mild overexpression accelerates aging with frequent symmetric cell divisions, despite no harmful effects on young cells. Our findings implicate that the interplay among these positive and negative polarity factors limits the life span of budding yeast. The American Society for Cell Biology 2022-03-11 /pmc/articles/PMC9250358/ /pubmed/35044837 http://dx.doi.org/10.1091/mbc.E21-04-0208 Text en © 2022 Kang et al. “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society for Cell Biology. https://creativecommons.org/licenses/by-nc-sa/3.0/This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial-Share Alike 4.0 International Creative Commons License. |
spellingShingle | Brief Reports Kang, Pil Jung Mullner, Rachel Li, Haoyu Hansford, Derek Shen, Han-Wei Park, Hay-Oak Up-regulation of the Cdc42 GTPase limits the replicative life span of budding yeast |
title | Up-regulation of the Cdc42 GTPase limits the replicative life span of budding yeast |
title_full | Up-regulation of the Cdc42 GTPase limits the replicative life span of budding yeast |
title_fullStr | Up-regulation of the Cdc42 GTPase limits the replicative life span of budding yeast |
title_full_unstemmed | Up-regulation of the Cdc42 GTPase limits the replicative life span of budding yeast |
title_short | Up-regulation of the Cdc42 GTPase limits the replicative life span of budding yeast |
title_sort | up-regulation of the cdc42 gtpase limits the replicative life span of budding yeast |
topic | Brief Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9250358/ https://www.ncbi.nlm.nih.gov/pubmed/35044837 http://dx.doi.org/10.1091/mbc.E21-04-0208 |
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